DL
Our Services

Pharmaceutical Trading Services Built for Compliance

Six core capabilities that carry a product from sourcing to shelf, managed by specialists at every stage.

Service 01

API Sourcing

We identify, audit and qualify active pharmaceutical ingredient manufacturers against WHO-GMP and international pharmacopoeia standards, giving partners confidence in every raw material batch.

  • Manufacturer audits and qualification
  • Certificate of Analysis verification on every lot
  • Therapeutic-category sourcing across generics and specialties
  • Alternate-source mapping to prevent supply disruption
Service 02

Contract Manufacturing

Our contract manufacturing programme manages finished-dose production end to end — formulation transfer, batch scheduling, in-process quality checks and release testing.

  • Tablets, capsules, oral liquids and injectables
  • Formulation and technology transfer support
  • In-process quality control checkpoints
  • Batch release documentation and CoA issuance
Service 03

Regulatory Affairs

Our regulatory affairs desk prepares and manages product dossiers, keeping registrations current across every market a partner operates in.

  • Common Technical Document (CTD) dossier preparation
  • Product registration and renewal filings
  • Post-approval variation management
  • Market-specific labelling and compliance review
Service 04

Global Export

We manage the documentation, customs coordination and shipping logistics that move compliant pharmaceutical products across borders reliably.

  • Export licensing and documentation
  • Customs clearance coordination
  • Cold-chain aware freight management
  • Landed-cost and lead-time transparency
Service 05

Supply Chain Management

From demand forecasting to warehousing, our supply chain team keeps partner inventories predictable and responsive to real demand.

  • Demand planning and forecast alignment
  • Inventory and warehousing coordination
  • Vendor performance monitoring
  • Order tracking and fulfilment visibility
Service 06

Product Registration

We manage the market-entry registration process so partners can launch compliant products without navigating unfamiliar regulatory frameworks alone.

  • Market entry regulatory strategy
  • Dossier compilation and submission
  • Liaison with local regulatory authorities
  • Registration timeline tracking
Common Questions

Frequently Asked

Answers to the questions we hear most often from new partners evaluating our services.

Every prospective partner undergoes a documented audit against WHO-GMP criteria, including facility inspection, quality system review and sample batch testing before onboarding.

Our regulatory affairs team currently manages active registrations across more than 38 countries, with dossier templates adapted to each region's requirements.

Yes. We work with partners on both trial-batch and full commercial volumes, scaling logistics and documentation accordingly.

Every export includes a Certificate of Analysis, Certificate of Origin, and all customs and regulatory documentation required by the destination market.

Not sure which service fits your requirement?

Share your requirement and our team will recommend the right service combination.

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